NDC 75834-326 – Methylphenidate Hydrochloride

Methylphenidate Hydrochloride 20 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC75834-326

Product details

Brand name
Methylphenidate Hydrochloride
Generic name
Methylphenidate Hydrochloride
Labeler
Nivagen Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA208737
Marketed since
April 16, 2024
Listing expires
December 31, 2026
Pharmacologic class
Central Nervous System Stimulant

Active ingredients

Uses, dosage, side effects and warnings for Methylphenidate Hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
75834-326-01100 TABLET in 1 BOTTLE (75834-326-01)Apr 16, 2024

Other Methylphenidate Hydrochloride products